EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at
Experience Project.
Joined: May 04, 2006 Posts: 3457 Location: Mid-Michigan
Posted: Fri Mar 09, 2007 10:40 am Post subject:
Thanks Dom,
And that is nice to hear.
Additionally, Ian has included links regarding Dr Scolding in the past, which I have read. I trust his knowledge, intelligence and outlook on MS.
Bob _________________ Wife diagnosed with RRMS in Feb. 2006.
Last edited by Lyon on Sun Mar 11, 2007 4:15 pm; edited 1 time in total
Joined: May 04, 2006 Posts: 3457 Location: Mid-Michigan
Posted: Fri Mar 09, 2007 12:27 pm Post subject:
viper498 wrote:
Bob,
Where is that information?
Hi Brock,
Are you referring to the information that Ian has sent, or Dom's link?
If you're talking about links that Ian has sent, here's a good one I was able to find quickly http://www.ezpresenter.net/msa/04.html Before clicking I should mention that it's audio/visual so you'll want to have a fast internet connection.
I have to admit that although I am known as a "computer geek" in these parts....I got a new computer about a month ago and spent a week or so getting it the way I wanted it...adding my favorite bookmarks and email addresses.
Two nights ago I thought I would "tweak it" by getting rid of unwanted and unused programs. I goofed things up so badly that I've had to re-install Vista and start from scratch last night and this morning.
I found the above link in my laptop but at the moment all my favorite bookmarks are history. If you search "Dr Neil Scolding" you'll find lots of info.
What I like about Dr Scolding is that he is just....well educated on the subject of ms and sensible. Dr Scolding reaffirms conclusions that I have come to although others might not be as impressed by him and might consider him too stodgey....conservative.
Bob _________________ Wife diagnosed with RRMS in Feb. 2006.
Joined: Jan 28, 2005 Posts: 735 Location: Northern Ontario, Canada
Posted: Fri Mar 09, 2007 2:07 pm Post subject:
It was good to see and hear what is going on inside me and us, for me the 50 years is to long though, it's to bad.. thx Forest and Lyon.. _________________ ~i guess i know i just hate how it sounds~
I see seven towers
But I only see one way out
Joined: May 04, 2006 Posts: 3457 Location: Mid-Michigan
Posted: Fri Mar 09, 2007 3:00 pm Post subject:
robbie wrote:
Slide 38..
Thanks robbie, I'll check it out. It's actually been months since I watched that presentation but I remember thinking that it was very informative and hopeful.
Well, I've gotten so that I like eating crow and having egg on my face.....You're right. I don't know what to say other than I'm MUCH more optomistic than that. The sound quality isn't real good. I'm going to listen again to make sure that he said 50 and not 15. I'm also going to try to find out when that presentation was. It might not be recent. Honestly robbie, things ARE MUCH more optomistic than that.
......"Page Info" says it was last modified on Friday, November 14, 2003 9:18:48 AM. I think it's safe to say that we've all seen reasons for vast improvement in optomism since then.
Bob _________________ Wife diagnosed with RRMS in Feb. 2006.
You cannot post new topics in this forum You cannot reply to topics in this forum You cannot edit your posts in this forum You cannot delete your posts in this forum You cannot vote in polls in this forum
We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project.
Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS,
on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!